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1000 Titel
  • The Intestinal Microbiota in Metabolic Disease
1000 Autor/in
  1. Woting, Anni |
  2. Blaut, Michael |
1000 Erscheinungsjahr 2016
1000 LeibnizOpen
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2016-04-06
1000 Erschienen in
1000 Quellenangabe
  • 8(4): 202
1000 FRL-Sammlung
1000 Copyrightjahr
  • 2016
1000 Lizenz
1000 Verlagsversion
  • http://dx.doi.org/10.3390/nu8040202 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4848671/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Gut bacteria exert beneficial and harmful effects in metabolic diseases as deduced from the comparison of germfree and conventional mice and from fecal transplantation studies. Compositional microbial changes in diseased subjects have been linked to adiposity, type 2 diabetes and dyslipidemia. Promotion of an increased expression of intestinal nutrient transporters or a modified lipid and bile acid metabolism by the intestinal microbiota could result in an increased nutrient absorption by the host. The degradation of dietary fiber and the subsequent fermentation of monosaccharides to short-chain fatty acids (SCFA) is one of the most controversially discussed mechanisms of how gut bacteria impact host physiology. Fibers reduce the energy density of the diet, and the resulting SCFA promote intestinal gluconeogenesis, incretin formation and subsequently satiety. However, SCFA also deliver energy to the host and support liponeogenesis. Thus far, there is little knowledge on bacterial species that promote or prevent metabolic disease. Clostridium ramosum and Enterococcus cloacae were demonstrated to promote obesity in gnotobiotic mouse models, whereas bifidobacteria and Akkermansia muciniphila were associated with favorable phenotypes in conventional mice, especially when oligofructose was fed. How diet modulates the gut microbiota towards a beneficial or harmful composition needs further research. Gnotobiotic animals are a valuable tool to elucidate mechanisms underlying diet–host–microbe interactions.
1000 Sacherschließung
lokal bile acids
lokal low-grade inflammation
lokal diet
lokal diabetes
lokal energy harvest
lokal SCFA
lokal absorption
lokal intestinal microbiota
lokal obesity
lokal metabolic syndrome
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1000 Förderer
  1. German Institute of Human Nutrition Potsdam-Rehbruecke |
1000 Fördernummer
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1000 Förderprogramm
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1000 Dateien
  1. The Intestinal Microbiota in Metabolic Disease
1000 Förderung
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    1000 Förderer German Institute of Human Nutrition Potsdam-Rehbruecke |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 Erstellt am 2017-08-28T15:21:09.829+0200
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